Canonical Allele Identifier: CA14937716
Gene: ZNRF3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.28904318C>T , CM000684.2:g.28904318C>T GRCh38
NC_000022.10:g.29300306C>T , CM000684.1:g.29300306C>T GRCh37
NC_000022.9:g.27630306C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000544604.7:c.300+20252C>T MANE Select ENSP00000443824.2:n.300+20252C>T
ENST00000544604.6:c.300+20252C>T ENSP00000443824.2:n.300+20252C>T
NM_001206998.1:c.300+20252C>T NP_001193927.1:n.300+20252C>T
XM_011530434.1:c.48+19207C>T XP_011528736.1:n.48+19207C>T
XM_011530435.1:c.15+82139C>T XP_011528737.1:n.15+82139C>T
XM_011530436.1:c.15+82139C>T XP_011528738.1:n.15+82139C>T
XM_011530437.1:c.15+82139C>T XP_011528739.1:n.15+82139C>T
XM_011530438.1:c.15+82139C>T XP_011528740.1:n.15+82139C>T
XM_011530440.1:c.-1+19288C>T XP_011528742.1:n.-1+19288C>T
XM_011530435.2:c.15+82139C>T XP_011528737.1:n.15+82139C>T
XM_011530436.3:c.15+82139C>T XP_011528738.1:n.15+82139C>T
XM_011530438.2:c.15+82139C>T XP_011528740.1:n.15+82139C>T
XM_017028990.1:c.15+82139C>T XP_016884479.1:n.15+82139C>T
NM_001206998.2:c.300+20252C>T MANE Select NP_001193927.1:n.300+20252C>T